Josep Gelpi

2009

• Synthesis, structural analysis, and biological evaluation of thioxoquinazoline derivatives as phosphodiesterase 7 inhibitors.

  ChemMedChem

  T. Castaño, H. Wang, N. E. Campillo, S. Ballester, C. González-García, J. Hernández, C. Pérez, J. Cuenca, A. Pérez-Castillo, A. Martínez, O. Huertas, J L. Gelpí, F J. Luque, H. Ke, and C. Gil
• Thienylhalomethylketones: irreversible glycogen synthase kinase 3 inhibitors as useful pharmacological tools

  D. I. Perez, S. Conde, C. Pérez, C. Gil, D. Simon, F. Wandosell, F. J. Moreno, J L. Gelpí, F J. Luque, and A. Martínez
• FlexServ: An integrated tool for the analysis of protein flexibility

  J. Camps, O. Carrillo, A. Emperador, L. Orellana, A. Hospital, M. Rueda, D. Cicin, M. D'Abramo, J L. Gelpí, and M. Orozco

2007

• Dissection of the Recognition Properties of p38 MAP Kinase. Determination of the Binding Mode of a New Pyridinyl−Heterocycle Inhibitor Family

  Journal of Medicinal Chemistry

  R. Soliva, J L. Gelpí, C. Almansa, M. Virgili, and M. Orozco
• Functional and structural characterization of the first prokaryotic member of the L-amino acid transporter (LAT) family: a model for APC transporters.

  The Journal of biological chemistry

  N. Reig, C. del Rio, F. Casagrande, M. Ratera, J L. Gelpí, D. Torrents, P. J. F. Henderson, H. Xie, S. A. Baldwin, A. Zorzano, D. Fotiadis, and M. Palacín
• A consensous view to Protein Dynamics

  M. Rueda, C. Ferrer, T. Meyer, A. Pérez, J. Camps, A. Hospital, J L. Gelpí, and M. Orozco
• Dissection of the recognition properties of p38 MAP Kinase. Determination of the binding mode of a new pyridinyl-heterocycle inhibitor family

  R. Soliva, J L. Gelpí, C. Almansa, M. Virgili, and M. Orozco

2006

• A fast method for the determination of fractional contributions to solvation in proteins

  D. Talavera, A. Morreale, A. Hospital, C. Ferrer-Costa, J L. Gelpí, X. de la Cruz, T. Meyer, R. Soliva, F J. Luque, and M. Orozco

2005

• Molecular Dynamics Extended Library

  J L. Gelpí
• SAR and 3D-QSAR Studies on thiadiaolidinones (TDZDs) derivatives: Esploration of structural requeriments as glycogen synthase kinase 3 (GSK-3) inhibitors

  J L. Gelpí, A. Martínez, A. Alonso, A. Castro, I. Dorronsoro, F J. Luque, C. Pérez, and F. J. Moreno